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3-Hydroxybenzyl alcohol → 3-(Pyridin-2-yloxy)benzaldehyde

HRID 1678582
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HRID 1678582 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][OH:6].Br[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][N:12]=1.C(=O)([O-])[O-].[K+].[K+]>N1C=CC=CC=1>[N:12]1[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=1[O:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1023-Hydroxybenzyl alcoholHCID 79732-BromopyridineHCID 11430Potassium Carbonate

생성물 1

HCID 27353633-(Pyridin-2-yloxy)benzaldehyde수율 61%

시약·촉매·용매 1

HCID 1049Pyridine용매

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온도
90 °C

실험 절차

3-Hydroxybenzyl alcohol (1.0 g, 8.2 mmol) was dissolved in pyridine (20 mL). 2-Bromopyridine (1.6 g, 9.8 mmol) and potassium carbonate (2.3 g, 16.4 mmol) were added thereto, and then the mixture was stirred at 90° C. for 10 minutes. Copper oxide(II) (1.6 g, 20.5 mmol) was further added thereto, and the reaction mixture was heated under reflux for 2 days. The reaction solution was filtered, and concentrated under reduced pressure. To the residue was added water, and the mixture was extracted with ethyl acetate. The extract was dried, and then concentrated under reduced pressure. The residue was purified with silica gel column chromatography (hexane/ethyl acetate=100:0 to 70:30) to give the title compound (1.0 mg, yield 61%).

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureunder reflux for 2 days
  3. filtrationThe reaction solution was filtered
  4. concentrationconcentrated under reduced pressure
  5. additionTo the residue was added water
  6. extractionthe mixture was extracted with ethyl acetate
  7. customThe extract was dried
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified with silica gel column chromatography (hexane/ethyl acetate=100:0 to 70:30)

출처 및 근거

ORD 기록
ord-6c30dd5c1b6f42d292cc86e16b1882fc
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08008525B2

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